DePaul University, Center for Community Research: Symptom Questionnaires

ahimsa

ahimsa

Senior Member (Voting Rights)
I thought it would be helpful to post a link to the DePaul University web page with their symptom questionnaires:

https://csh.depaul.edu/about/center...gic-encephalomyelitis-cfs/Pages/measures.aspx
DePaul Symptom Questionnaires are below:

These are our questionnaires for measuring symptoms of ME/CFS, ME, and COVID-19. Psychometric properties of our surveys are cited below. All instruments are free to use. If you are considering translating any of our surveys, please let us know as we would be happy to provide you with helpful suggestions.
Click to expand...
 
ahimsa said:
I thought it would be helpful to post a link to the DePaul University web page with their symptom questionnaires:

https://csh.depaul.edu/about/center...gic-encephalomyelitis-cfs/Pages/measures.aspx
Click to expand...
Thanks so much, @ahimsa . Is this questionnaire widely used? I'll have an appointment with a doctor who is seeing lots of ME/CFS patients and I am really not sure what to expect.

I've seen a neurologist before who said I have CFS, but I'm not sure what a doctor who says to have a 'special interest' in ME/CFS would use for diagnosis.

I might post this as a separate thread, but I'll see how far I'll get here. :)
 
Thread to discuss latest PEM questionnaire here
Trish

Open Thread 'DSQ PEM survey - DePaul University, open October 2025'

Copy of Facebook post by Leonard Jason:

From the DePaul Group:

Are you 18 or older? Do you experience Post-Exertional Malaise? Or are you a member of the general population interested in contributing to research?

We are conducting a brief online survey as part of a research study focused on Post-Exertional Malaise (PEM). Your responses will help us evaluate the validity and reliability of a new survey tool designed to assess PEM symptoms.

The survey takes approximately 10-15 minutes to complete. Participation is entirely voluntary and anonymous. Additional information is...
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